Keith Richard Fandrick
Affiliations: | 2007 | Harvard University, Cambridge, MA, United States |
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"Keith Fandrick"Mean distance: 7.65
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Sign in to add mentor| David A. Evans | grad student | 2007 | Harvard | |
| (Asymmetric Friedel -Crafts alkylations catalyzed by bis(oxazolinyl)pyridine -scandium(III) triflate complexes.) | ||||
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| Patel ND, Sieber JD, Tcyrulnikov S, et al. (2018) Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki-Miyaura and Negishi Cross-Coupling Reactions for Tetra-Substituted Biaryl Synthesis. Acs Catalysis. 8: 10190-10209 |
| Qu B, Mangunuru HPR, Tcyrulnikov S, et al. (2018) Enantioselective Synthesis of α-(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights. Organic Letters |
| Zou Y, Gutierrez O, Sader AC, et al. (2017) A Computational Investigation of the Ligand-Controlled Cu-Catalyzed Site-Selective Propargylation and Allenylation of Carbonyl Compounds. Organic Letters |
| Han ZS, Wu H, Xu Y, et al. (2017) General and Stereoselective Method for the Synthesis of Sterically Congested and Structurally Diverse P-Stereogenic Secondary Phosphine Oxides. Organic Letters |
| Lautens M, Johnson T, Fandrick DR, et al. (2017) Copper-Catalyzed Propargylation of Cyclic Aldimines Synfacts. 13: 169-169 |
| Haddad N, Mangunuru HPR, Fandrick KR, et al. (2017) Ligand Effect on Diastereoselectivity in Suzuki–Miyaura Coupling Synfacts. 13: 168-168 |
| Mulder JA, Gao J, Fandrick KR, et al. (2017) Early Development Scale-Up of a Structurally-Challenging 5-Lipoxygenase Activating Protein (FLAP) Inhibitor Organic Process Research & Development. 21: 1427-1434 |
| Patel ND, Rivalti D, Buono FG, et al. (2017) Effective BI-DIME Ligand for Suzuki-Miyaura Cross-Coupling Reactions in Water with 500 ppm Palladium Loading and Triton X Asian Journal of Organic Chemistry. 6: 1285-1291 |
| Fandrick DR, Hart CA, Okafor IS, et al. (2016) Copper-Catalyzed Asymmetric Propargylation of Cyclic Aldimines. Organic Letters. 18: 6192-6195 |
| Wei X, Qu B, Zeng X, et al. (2016) Sequential C-H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor. Journal of the American Chemical Society |